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Therapeutic time window of Ad-GDNF after transient middle cerebral artery occlusion in rat

机译:大鼠瞬时中脑动脉闭塞后AD-GDNF治疗时间窗

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Time-dependent influence of adenovims-mediated glial cell line-derived neurotrophic factor (GDNF) gene (Ad-GDNF) was examined after 90 min of transient middle cerebral artery occlusion (MCAO) in rats. Treatment with Ad-GDNF significantly reduced the infarct volume when immediately administered after reperfusion, but became insignificant when administered at 1 h after the reperfusion as were the cases treated with vehicle and adenoviral vector containing the Escherichia coli lacZ gene (Ad-LacZ)-treated groups. The protective effect of GDNF was related to the significant reduction of the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin in situ nick end labeling (TUNEL)-positive cells as well as immunohistochemical positive cells for active caspase-3 but not caspase-9.These results showed that exogenous GDNF gene transfer successfully reduced the infarct size in a time-dependant manner by suppressing active caspase-3 but not active caspase-9. However, the therapeutic time window was shorter than the effect of GDNF protein itself previously reported.
机译:在大鼠瞬时中间脑动脉闭塞(MCAO)的90分钟后,检查腺过热症介导的腺内介导的神经胶质细胞系衍生的神经营养因子(GDNF)基因(AD-GDNF)的时间依赖性影响。当再灌注后立即给药时,用Ad-GDNF治疗显着降低了梗塞体积,但在再灌注后在1小时内施用时,含有载体和腺病毒载体(Ad-LacZ)-Treated的血管病毒载体(Ad-LacZ)治疗的病例而变得微不足道团体。 GDNF的保护作用与原位缺口末端标记(TUNEL) - 阳性细胞的终末脱氧核苷酸转移酶介导的DUTP-BIOTIN的数量的显着降低有关,以及活性胱天蛋白酶-3的免疫组化阳性细胞,但不是Caspase-9这些结果表明,外源性GDNF基因转移通过抑制活性半胱天冬酶-3但不活性的Caspase-9成功地以时间依赖性方式降低了梗塞尺寸。然而,治疗时间窗短于先前GDNF蛋白本身的效果短。

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